WO2012124307A1 - Préimprégné pour circuit multicouche - Google Patents

Préimprégné pour circuit multicouche Download PDF

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Publication number
WO2012124307A1
WO2012124307A1 PCT/JP2012/001685 JP2012001685W WO2012124307A1 WO 2012124307 A1 WO2012124307 A1 WO 2012124307A1 JP 2012001685 W JP2012001685 W JP 2012001685W WO 2012124307 A1 WO2012124307 A1 WO 2012124307A1
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WO
WIPO (PCT)
Prior art keywords
resin
prepreg
weight
layer
laminated
Prior art date
Application number
PCT/JP2012/001685
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English (en)
Japanese (ja)
Inventor
忠相 遠藤
保明 三井
Original Assignee
住友ベークライト株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2011055195A external-priority patent/JP5579642B2/ja
Priority claimed from JP2011055198A external-priority patent/JP5547678B2/ja
Application filed by 住友ベークライト株式会社 filed Critical 住友ベークライト株式会社
Priority to CN2012800133337A priority Critical patent/CN103444276A/zh
Priority to KR1020137026779A priority patent/KR101907713B1/ko
Publication of WO2012124307A1 publication Critical patent/WO2012124307A1/fr

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    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00—Apparatus or processes for manufacturing printed circuits
    • H05K3/46—Manufacturing multilayer circuits
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C08J5/0405—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres
    • C08J5/043—Reinforcing macromolecular compounds with loose or coherent fibrous material with inorganic fibres with glass fibres
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
    • C08J5/241—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres
    • C08J5/244—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using inorganic fibres using glass fibres
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00—Layered products comprising a layer of metal
    • B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/12—Layered products comprising a layer of synthetic resin next to a fibrous or filamentary layer
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
    • C08J5/249—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs characterised by the additives used in the prepolymer mixture
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00—Printed circuits
    • H05K1/02—Details
    • H05K1/03—Use of materials for the substrate
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K1/00—Printed circuits
    • H05K1/02—Details
    • H05K1/03—Use of materials for the substrate
    • H05K1/0313—Organic insulating material
    • H05K1/0353—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement
    • H05K1/0366—Organic insulating material consisting of two or more materials, e.g. two or more polymers, polymer + filler, + reinforcement reinforced, e.g. by fibres, fabrics
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
    • H05K3/00—Apparatus or processes for manufacturing printed circuits
    • H05K3/46—Manufacturing multilayer circuits
    • H05K3/4644—Manufacturing multilayer circuits by building the multilayer layer by layer, i.e. build-up multilayer circuits
    • H05K3/4673—Application methods or materials of intermediate insulating layers not specially adapted to any one of the previous methods of adding a circuit layer
    • H05K3/4676—Single layer compositions
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins

Definitions

  • the present invention relates to a prepreg for buildup.
  • a manufacturing technique of a laminated wiring board by a build-up method in which insulating layers and conductor layers are alternately stacked on a circuit board is known.
  • Patent Document 1 a laminate material composed of a prepreg and a metal foil impregnated with a thermosetting resin varnish on a paper or cloth base material is sandwiched between mirror plates, and a large number of layers are laminated, and a cushion material and a carrier material are interposed.
  • the cushion material has protrusions along each side formed on the surface side thereof.
  • the manufacturing method of the thermosetting resin laminated board characterized by this is described. According to this method, since the protrusions along the sides are formed on the surface of the cushion material, the pressure at the outer peripheral edge of the laminated material is higher than that at the other parts during press molding, It is said that this resin hardly protrudes to the outside.
  • Patent Document 2 discloses a resin composition layer surface of an adhesive film composed of a support base film and a resin composition layer on a patterned circuit board using a vacuum laminating apparatus that can be heated and pressurized.
  • a vacuum laminating apparatus that can be heated and pressurized.
  • an anti-smudge sheet smaller than the surface area of the adhesive film is provided between at least one press plate of the vacuum laminating apparatus and the support base film surface of the adhesive film, and the anti-smudge sheet is provided around the surface of the adhesive film.
  • Patent Document 3 discloses that a technical problem is to provide a prepreg suitable for a polyphenylene ether laminate without micro-undulation, and means for solving the technical problem is described as “thermosetting polyphenylene ether resin composition”.
  • a prepreg formed by combining a product and a substrate it is described that a prepreg characterized by having a resin flow of 1% to 25% is described.
  • Patent Document 3 discloses a technique based on a prepreg formed by combining a thermosetting polyphenylene ether resin composition and a substrate, and includes a prepreg having a resin layer not containing polyphenylene ether. Is not listed.
  • the one described in Patent Document 3 has a drawback that a copper-clad laminate made of an epoxy resin has poor electrical characteristics, particularly dielectric characteristics in a high frequency region. Polyphenylene ether is used as a material for solving this problem. Attention is focused on application to copper-clad laminates. Therefore, the thing of patent document 3 cannot be used for the technique of a prepreg provided with the resin layer containing the thermosetting resin which has an epoxy resin as a main component.
  • the resin flow and the type of the resin composition constituting the resin layer are inseparable.
  • the resin flow is a parameter determined by a balance between the viscosity of the resin and the progress of the reaction of the resin.
  • the polyphenylene ether resin has a high viscosity, and a good inner layer circuit embedding property cannot be obtained by the prepreg provided with the resin layer containing the polyphenylene ether resin.
  • the present invention has been made in view of the above circumstances, and an object of the present invention is to provide a build-up prepreg that achieves both improvement in embedding of an inner layer circuit and improvement in thickness accuracy.
  • a fiber base and a resin layer provided on both sides of the fiber base According to IPC-TM-650 Method 2.3.17, the resin flow measured by heating and pressurizing for 5 minutes under the conditions of 171 ⁇ 3 ° C. and 1380 ⁇ 70 kPa is 15 wt% or more and 50 wt% or less.
  • a build-up prepreg is provided.
  • the build-up prepreg of the present invention contains a thermosetting resin in the resin layer,
  • the thermosetting resin is preferably selected from an epoxy resin, a cyanate resin, and a maleimide compound.
  • a prepreg for buildup that can achieve both improvement in embedding property of an inner layer circuit and improvement in thickness accuracy.
  • the prepreg according to the present invention is a prepreg for buildup including a fiber base material and resin layers provided on both surfaces of the fiber base material.
  • This prepreg is based on IPC-TM-650 Method 2.3.17, and the resin flow measured by heating and pressurizing for 5 minutes under the conditions of 171 ⁇ 3 ° C. and 1380 ⁇ 70 kPa is 15% by weight to 50% by weight. It is as follows. By setting the resin flow measured under the above conditions to 15% by weight or more, a prepreg excellent in the embedding property of the inner layer circuit can be obtained.
  • the upper limit of the resin flow is 50% by weight or less, the outflow of the resin layer from the prepreg can be suppressed when the prepreg is laminated and pressed. Therefore, when it is laminated on the core layer having the circuit forming surface, it is possible to realize a build-up prepreg that is excellent in embedding of the inner layer circuit and that can suppress the outflow of the resin layer from the prepreg during the lamination press.
  • the prepreg according to the present invention protrudes from the outer edge of the fiber base material in a plan view when heated and pressed under the conditions of 120 ° C. and 2.5 MPa with the pair of opposed rubber plates sandwiched between the prepregs.
  • the weight of the resin layer is preferably 5% by weight or less with respect to the entire resin layer.
  • FIG. 1 is a diagram showing an example of a prepreg of the present invention.
  • the prepreg 1 includes a fiber base 2 and resin layers 3 and 4 that are provided on both sides of the fiber base 2 and contain a thermosetting resin.
  • the prepreg 1 can be formed by impregnating the fiber base 2 with a resin composition.
  • the resin composition P used for the prepreg 1 is demonstrated, the resin composition which comprises the resin layers 3 and 4 may mutually be the same, and may differ, respectively.
  • the resin composition P used for the prepreg 1 contains (A) a thermosetting resin.
  • the thermosetting resin is selected from an epoxy resin, a cyanate resin, and a maleimide compound, and can include one or more of these.
  • the content of the thermosetting resin in the resin composition P is not particularly limited, but is preferably 15 to 80% by weight, more preferably 25 to 50% by weight, based on the entire resin composition P.
  • epoxy resin examples include bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, bisphenol E type epoxy resin, bisphenol M type epoxy resin, bisphenol P type epoxy resin, and bisphenol Z type epoxy resin.
  • novolac type epoxy resin novolac type epoxy resin, biphenyl type epoxy resin, biphenyl aralkyl type epoxy resin etc., arylalkylene type epoxy resin, naphthalene type epoxy resin, anthracene type epoxy resin , Phenoxy type epoxy resin, dicyclopentadiene type epoxy resin, norbornene type epoxy resin, adamantane type epoxy resin, fluorene
  • epoxy resins such as type epoxy resin.
  • One of these can be used alone, or two or more can be used in combination.
  • the content of the epoxy resin is not particularly limited, but is preferably 15 to 80% by weight of the entire resin composition P. More preferably, it is 25 to 50% by weight.
  • a liquid epoxy resin such as a liquid bisphenol A type epoxy resin or a bisphenol F type epoxy resin because the impregnation property to the fiber base material can be improved.
  • the content of the liquid epoxy resin is more preferably 3 to 14% by weight based on the entire resin composition P.
  • adhesion to the conductor can be improved.
  • cyanate resin Although it does not specifically limit as a kind of cyanate resin, for example, novolak type cyanate resin, naphthol aralkyl type cyanate resin, dicyclopentadiene type cyanate resin, biphenyl type cyanate resin, bisphenol A type cyanate resin, bisphenol E type cyanate resin, tetramethyl Examples thereof include bisphenol type cyanate resins such as bisphenol F type cyanate resins. Among these, phenol novolac type cyanate resin is preferable from the viewpoint of low thermal expansion. Furthermore, other cyanate resins may be used alone or in combination of two or more, and are not particularly limited. The cyanate resin is preferably 8 to 20% by weight of the entire resin composition P.
  • maleimide compounds include bismaleimide and bismaleimide / triazine resin (BT resin) composed of bismaleimide and cyanate ester.
  • bismaleimide examples include 4,4′-diphenylmethane bismaleimide, m-phenylene bismaleimide, p-phenylene bismaleimide, 2,2 ′-[4- (4-maleimidophenoxy) phenyl] propane, bis- (3 -Ethyl-5-methyl-4-maleimidophenyl) methane, 4-methyl-1,3-phenylenebismaleimide, N, N'-ethylenedimaleimide, N, N'-hexamethylenedimaleimide and the like.
  • the maleimide compound is preferably 20% by weight or less of the entire resin composition P.
  • the resin composition P preferably contains (B) a filler.
  • silica is more preferable, and fused silica (particularly spherical fused silica) is particularly preferable in terms of excellent low thermal expansion.
  • fused silica particularly spherical fused silica
  • the shape is crushed and spherical, but in order to reduce the melt viscosity of the resin composition P in order to ensure the impregnation of the fiber base material, a method of use according to the purpose such as using spherical silica is adopted.
  • the average particle diameter of the filler is not particularly limited, but is preferably 0.01 to 3 ⁇ m, particularly preferably 0.02 to 1 ⁇ m.
  • a varnish can be made low viscosity and the fiber composition can be made to impregnate the resin composition P favorably.
  • sedimentation etc. of (B) filler can be suppressed in a varnish.
  • This average particle diameter can be measured by, for example, a particle size distribution meter (manufactured by Shimadzu Corporation, product name: laser diffraction particle size distribution measuring device SALD series).
  • the (B) filler is not particularly limited, but a monodispersed filler having an average particle diameter can be used, and a filler having a polydispersed average particle diameter can be used. Furthermore, one type or two or more types of fillers having an average particle size of monodisperse and / or polydisperse can be used in combination.
  • spherical silica (especially spherical fused silica) having an average particle size of 3 ⁇ m or less is preferable, and spherical fused silica having an average particle size of 0.02 to 1 ⁇ m is particularly preferable. Thereby, the filling property of the (B) filler can be improved.
  • the content of the filler is not particularly limited, but is preferably 2 to 70% by weight, and particularly preferably 5 to 60% by weight, based on the entire resin composition P. When the content is within the above range, particularly low thermal expansion and low water absorption can be achieved. If necessary, the resin layers 3 and 4 can change the content of the (B) filler to achieve both adhesion to the conductor and low thermal expansion.
  • the resin composition P used for the prepreg 1 is not particularly limited, but preferably contains (C) a coupling agent.
  • (C) Coupling agent improves the wettability of the interface between (A) thermosetting resin and (B) filler, thereby allowing (A) thermosetting resin and (B ) It is possible to fix the filler uniformly and improve the heat resistance, particularly the solder heat resistance after moisture absorption.
  • any coupling agent can be used as long as it is usually used. Specifically, an epoxy silane coupling agent, a cationic silane coupling agent, an amino silane coupling agent, a titanate coupling agent, and a silicone oil type. It is preferable to use one or more coupling agents selected from coupling agents. Thereby, the wettability with the interface of (B) filler can be made high, and thereby heat resistance can be improved more.
  • the amount of the coupling agent (C) is not particularly limited because it depends on the specific surface area of the (B) filler, but is preferably 0.05 to 3 parts by weight with respect to 100 parts by weight of the (B) filler. 0.1 to 2 parts by weight is preferred.
  • (C) By making the content of the coupling agent 0.05 parts by weight or more with respect to 100 parts by weight of (B) filler, (B) the filler can be sufficiently covered, and heat resistance can be improved. it can.
  • (C) By making content of a coupling agent into 3 weight part or less with respect to 100 weight part of (B) fillers, reaction advances favorably and decline in bending strength etc. can be prevented.
  • Resin composition P may further contain (D) a phenol-based or amine-based curing agent.
  • a phenol-based or amine-based curing agent known or commonly used phenolic novolac resins, alkylphenol novolac resins, bisphenol A novolac resins, dicyclopentadiene type phenol resins, zyloc type phenol resins, terpene modified phenol resins, polyvinylphenols, etc. Can be used in combination.
  • aromatic amines such as 3,3′-diethyl-4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenylmethane, and diethyltoluenediamine may be used alone or in combination of two or more. it can.
  • the compounding amount of the phenol curing agent is (A) when the epoxy resin is included as the thermosetting resin, the equivalent ratio with the epoxy resin (phenolic hydroxyl group equivalent / epoxy group equivalent) is 0.1 to 1.0. Preferably there is. As a result, there remains no unreacted phenol curing agent, and the moisture absorption heat resistance is improved.
  • the compounding amount of the amine curing agent is preferably 0.1 to 2.0 in an equivalent ratio with (A) the thermosetting resin.
  • the resin composition P may contain (E) a curing accelerator as necessary.
  • E A well-known thing can be used as a hardening accelerator.
  • organic metal salts such as zinc naphthenate, cobalt naphthenate, tin octylate, cobalt octylate, bisacetylacetonate cobalt (II), trisacetylacetonate cobalt (III), triethylamine, tributylamine, diazabicyclo [2,2 , 2] tertiary amines such as octane, 2-phenyl-4-methylimidazole, 2-ethyl-4-ethylimidazole, 2-phenyl-4-methylimidazole, 2-phenyl-4-methyl-5-hydroxyimidazole Imidazoles such as 2-phenyl-4,5-dihydroxyimidazole, phenol compounds such as phenol, bisphenol A, and nonylphenol, organic acids such as acetic acid
  • the content of the curing accelerator is not particularly limited, but is preferably 0.05 to 5% by weight, particularly preferably 0.2 to 2% by weight, based on the entire resin composition P.
  • the content is preferably 0.05 to 5% by weight, particularly preferably 0.2 to 2% by weight, based on the entire resin composition P.
  • the resin composition P is composed of a thermoplastic resin such as phenoxy resin, polyimide resin, polyamideimide resin, polyamide resin, polyethersulfone resin, polyester resin, polyethylene resin, polystyrene resin, styrene-butadiene copolymer, styrene-isoprene copolymer.
  • a thermoplastic resin such as phenoxy resin, polyimide resin, polyamideimide resin, polyamide resin, polyethersulfone resin, polyester resin, polyethylene resin, polystyrene resin, styrene-butadiene copolymer, styrene-isoprene copolymer.
  • thermoplastic elastomers such as polystyrene-based thermoplastic elastomers, polyolefin-based thermoplastic elastomers, polyamide-based elastomers, polyester-based elastomers, and diene-based elastomers such as polybutadiene, epoxy-modified polybutadiene, acrylic-modified polybutadiene, and methacryl-modified polybutadiene May be.
  • addition of the above components such as pigments, dyes, antifoaming agents, leveling agents, ultraviolet absorbers, foaming agents, antioxidants, flame retardants, ion scavengers, etc. A thing may be added.
  • the fiber substrate 2 impregnated with the resin composition P is not particularly limited, but glass fiber substrates (glass cloth) such as glass woven fabric and glass nonwoven fabric, polyamide resin fibers, aromatic polyamide resin fibers, wholly aromatic polyamide resins.
  • Main components are polyamide resin fibers such as fibers, polyester resin fibers, aromatic polyester resin fibers, polyester resin fibers such as wholly aromatic polyester resin fibers, polyimide resin fibers, polybenzoxazole resin fibers, and fluororesin fibers.
  • Examples thereof include organic fiber substrates such as synthetic fiber substrates composed of woven fabrics or nonwoven fabrics, kraft paper, cotton linter paper, paper substrates mainly composed of linter and kraft pulp mixed paper, and the like.
  • glass cloth is preferable. Thereby, a prepreg having low water absorption, high strength, and low thermal expansion can be obtained.
  • Examples of the glass constituting the glass cloth include E glass, C glass, A glass, S glass, D glass, NE glass, T glass, H glass, and Q glass.
  • E glass or T glass is preferable. Thereby, the high elasticity of a prepreg can be achieved and the thermal expansion coefficient of a prepreg can be reduced.
  • the method of impregnating the fiber base material 2 with the resin composition P includes, for example, a method of preparing the resin varnish V using the resin composition P, immersing the fiber base material 2 in the resin varnish V, and a method of applying with various coaters And a method of spraying by spraying.
  • the method of immersing the fiber base material 2 in the resin varnish V is preferable.
  • the impregnation property of the resin composition P with respect to the fiber base material 2 can be improved.
  • a normal impregnation coating equipment can be used.
  • the solvent used for the resin varnish V desirably has good solubility in the resin component in the resin composition P, but a poor solvent may be used as long as it does not adversely affect the resin varnish V.
  • the solvent exhibiting good solubility include acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone, cyclopentanone, tetrahydrofuran, dimethylformamide, dimethylacetamide, dimethyl sulfoxide, ethylene glycol, cellosolve, and carbitol.
  • the solid content of the resin varnish V is not particularly limited, but the solid content of the resin composition P is preferably 20 to 80% by weight, particularly preferably 35 to 65% by weight. Thereby, the impregnation property to the fiber base material of the resin varnish V can further be improved.
  • the predetermined temperature at which the fiber base material 2 is impregnated with the resin composition P is not particularly limited.
  • the prepreg 1 can be obtained by drying at 90 to 220 ° C. or the like.
  • the thickness of the prepreg 1 is preferably 20 to 100 ⁇ m.
  • the prepreg 1 may have a relatively thick resin layer 3 and a relatively thin resin layer 4 with the fiber substrate 2 as the center, and the fiber substrate 2 as the center. You may have the resin layer which consists of substantially the same thickness.
  • the center 5 in the thickness direction of the fiber base material may be shifted from the center 6 in the thickness direction of the prepreg.
  • the thickness of the resin layers 3 and 4 is the first surface of the prepreg 1 from the thickness center 5 of the fiber substrate in the sectional view of the prepreg 1 shown in FIG.
  • T1 is the thickness of the thick resin layer 3 and T2 is the thickness of the thin resin layer 4.
  • the second surface S2 is a surface opposite to the first surface S1.
  • T1 / T2 is preferably 1 or more and 5 or less, more preferably 1.5 or more and 4.5 or less, and further preferably 2 or more and 4 or less.
  • the prepreg 1 can be evaluated by measuring the resin flow measured by heating and pressurizing for 5 minutes under the conditions of 171 ⁇ 3 ° C. and 1380 ⁇ 70 kPa in accordance with IPC-TM-650 Method 2.3.17. it can.
  • the resin flow of the prepreg 1 is 15% by weight or more, a prepreg excellent in embedding of the wiring circuit can be obtained. Moreover, if this resin flow is 50 weight% or less, when the prepreg is laminated and pressed, the outflow of the resin composition P can be suppressed.
  • the upper limit is preferably 40% by weight or less, and more preferably 35% by weight or less. By carrying out like this, the thickness uniformity of the laminated board obtained by building up the prepreg 1 can be improved.
  • the resin flow can be increased by reducing the average molecular weight of a thermosetting resin such as an epoxy resin contained in the resin composition P used in the prepreg 1. Moreover, resin flow can be made small by increasing the content of the filler contained in the resin composition P used for the prepreg 1.
  • a thermosetting resin such as an epoxy resin contained in the resin composition P used in the prepreg 1.
  • the performance of the prepreg 1 for buildup can be evaluated as follows. That is, when the prepreg 1 is placed between two metal plates and pressed for 60 seconds through a rubber plate under the conditions of 120 ° C. and 2.5 MPa, the resin layer 3 protrudes from the outer edge of the fiber substrate 2 in plan view, Measure the weight of 4. At this time, the size of the prepreg 1 in plan view is 200 mm ⁇ 200 mm.
  • the metal plate SUS having a thickness of 1.5 mm is used.
  • the rubber plate is made of silicon rubber having a rubber hardness measured in accordance with JIS K 6253 A of 60 ° and a thickness of 3 mm.
  • Thickness uniformity of the laminate obtained by building up the prepreg 1 by setting the protruding amount of the resin layers 3 and 4 thus measured to 5% by weight or less with respect to the entire resin layers 3 and 4. Can be improved. There is no particular lower limit, and it is preferably 0% by weight or more with respect to the entire resin layers 3 and 4.
  • the amount of protrusion of the resin layers 3 and 4 increases. Moreover, the amount of protrusion of the resin layers 3 and 4 can be reduced by blending or increasing the polymer resin having a weight average molecular weight exceeding 10,000, such as the phenoxy resin contained in the resin composition P used in the prepreg 1. can do.
  • the prepreg 1 may be a laminate of a plurality of sheets via metal foil or film.
  • Metal foils include, for example, copper and copper alloys, aluminum and aluminum alloys, silver and silver alloys, gold and gold alloys, zinc and zinc alloys, nickel and nickel alloys, tin and tin alloys, iron and iron Examples thereof include metal foils such as alloy alloys. Of these, copper foil is preferred.
  • heating and pressurization may be performed.
  • the heating temperature is not particularly limited, but is preferably 120 to 230 ° C, and particularly preferably 150 to 210 ° C.
  • the pressure to be applied is not particularly limited, but is preferably 1 to 5 MPa, and particularly preferably 2 to 4 MPa.
  • the prepreg 1 may be wound and laminated in a roll shape.
  • a support base material may be provided on one side or both sides, and the support base material may be wound and laminated. Examples of the method of winding and laminating the prepreg 1 in a roll shape include the following.
  • the fiber base material 2 After impregnating the fiber base material 2 with the resin composition P, it is transported to the roll type laminating apparatus together with the supporting base material, and the supporting base material is continuously pressed and heated on the prepreg 1 with a metal roll or an elastic material roll. Laminate by. Then, the prepreg 1 can be wound and laminated
  • a plastic film can be used as the support substrate.
  • polyesters such as polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), polycarbonate (PC), acrylic resin (PMMA), cyclic polyolefin, triacetyl cellulose ( TAC), polyether sulfide (PES), polyether ketone, polyimide and the like.
  • PET polyethylene terephthalate
  • PEN polyethylene naphthalate
  • PC polycarbonate
  • acrylic resin PMMA
  • cyclic polyolefin triacetyl cellulose
  • TAC triacetyl cellulose
  • PES polyether sulfide
  • polyether ketone polyimide and the like.
  • the support substrate may be subjected to mat treatment or corona treatment on the laminated surface of the resin layers 3 and 4.
  • a release layer may be provided on the surface in contact with the prepreg 1.
  • a protective material may be provided on the other side.
  • it is conveyed to a roll type laminating apparatus so that the supporting surface is in contact with the second surface S2 and the protective material is in contact with the first surface S1, and a metal roll or an elastic material roll is formed from both the supporting substrate and the protective material.
  • a protective material for example, polyolefins such as polyethylene, polypropylene, and polyvinyl chloride, polyesters such as PET and PEN, and plastic films such as PC and polyimide can be used.
  • the thickness of the protective material is preferably in the range of 5 to 30 ⁇ m.
  • the laminate includes a core layer having a circuit formation surface on one side or both sides, and a build-up layer laminated on the circuit formation surface of the core layer.
  • the build-up layer is formed by curing the prepreg 1 described above.
  • the core layer is a sheet-like thing having a circuit forming surface in which one side or both sides of a substrate such as a glass epoxy substrate, a metal substrate, a polyester substrate, a polyimide substrate, a BT resin substrate, and a thermosetting polyphenylene ether substrate are patterned.
  • the core layer further includes an inner layer circuit board of an intermediate product on which a buildup layer and a wiring circuit are to be formed.
  • the manufacturing method of the core layer is not particularly limited.
  • a core layer having a metal foil on both sides is used, a predetermined place is opened with a drill machine, and the both sides of the core layer are made conductive by electroless plating. .
  • the inner layer circuit is formed by etching the metal foil.
  • the inner layer circuit portion can be suitably used after being subjected to roughening processing such as blackening processing.
  • the opening can be appropriately filled with a conductor paste or a resin paste.
  • This laminate can be manufactured as follows. First, a prepreg 1 wound in a roll shape is prepared and conveyed to a laminator together with the sheet-shaped core layer.
  • the laminator includes a pair of opposing metal plates and a plate-like elastic body such as a heat insulating rubber, and is heated and pressurized by the metal plate with the core layer and the prepreg sandwiched through the elastic body, Lamination (lamination process).
  • a laminator vacuum laminator
  • the metal plate for example, a SUS end plate can be used. Heating and pressing are preferably performed in the range of 80 to 140 ° C. and 0.4 to 1.5 MPa.
  • the above laminator step can be performed using a commercially available vacuum laminator.
  • a vacuum pressurization type laminator provided in Nichigo-Morton CPV300 or an equivalent thereof can be used.
  • the laminated adhesive sheet is smoothed by hot pressing the laminated buildup layer and the core layer with a pair of opposing metal plates (smoothing step).
  • the smoothing step is performed by heating and pressurizing the adhesive sheet with a metal plate such as a heated SUS mirror plate under atmospheric pressure.
  • the smoothing press is preferably performed in the range of 100 to 170 ° C. and 0.4 to 1.5 MPa.
  • Such a smoothing step can be performed using a commercially available hot press apparatus.
  • a hot press apparatus provided in a CPV300 manufactured by Nichigo-Morton Co., Ltd. or an equivalent thereof may be used. it can.
  • the curing temperature is not particularly limited.
  • the curing can be performed within a range of 100 to 250 ° C., and preferably 150 to 200 ° C.
  • the curing time can be about 30 to 75 minutes.
  • the cured resin layer is irradiated with a laser to form an opening, and the resin residue after the laser irradiation is preferably removed with an oxidizing agent such as permanganate or dichromate.
  • an oxidizing agent such as permanganate or dichromate.
  • the surface of the smooth resin layer can be simultaneously roughened, and the adhesion of the conductive wiring circuit formed by subsequent metal plating can be improved.
  • the resin layer can be uniformly provided with fine irregularities in the roughening treatment.
  • a fine wiring circuit can be formed with high accuracy.
  • a solder resist is formed on the outermost layer, the connection electrode part is exposed so that a semiconductor element can be mounted by exposure and development, nickel gold plating is performed, and the laminate is cut to a predetermined size. .
  • the resin amount of the prepreg 1 is different between the first surface S1 side and the second surface S2 side, that is, when T1> T2 in FIG. 1, the first surface S1 with a large amount of resin is the circuit forming surface. It is preferable to be laminated. By carrying out like this, resin can fully be supplied to the space
  • This semiconductor device can be manufactured by mounting a semiconductor element on the laminated wiring board.
  • the mounting method and the sealing method of the semiconductor element are not particularly limited. For example, it can be manufactured by the following method.
  • connection electrode part on the laminated wiring board is aligned with the solder bumps of the semiconductor element.
  • solder bump is heated to the melting point or higher by using an IR reflow device, a hot plate, or other heating device, and the multilayer printed wiring board and the solder bump are connected by fusion bonding.
  • a liquid sealing resin is filled between the laminated wiring board and the semiconductor element and cured to obtain a semiconductor device.
  • the prepreg shown in FIG. 1 was produced.
  • the raw materials used in Examples and Comparative Examples are as follows.
  • Inorganic filler spherical silica (manufactured by Admatechs, SO-25R, average particle size 0.5 ⁇ m)
  • Inorganic filler Boehmite (Navaltech, AOH-30)
  • Organic filler Silicone particles (manufactured by Shin-Etsu Chemical Co., Ltd., KMP600, average particle size 5 ⁇ m)
  • Epoxy resin Biphenyl aralkyl type novolac epoxy resin (Nippon Kayaku Co., Ltd., NC-3000)
  • Epoxy resin dicyclopentadiene type novolac epoxy resin (manufactured by DIC, HP-7200L, HP-7200)
  • Epoxy resin Bisphenol A type liquid epoxy resin (Mitsubishi Chemical Corporation, jER-828)
  • Epoxy resin Bisphenol F type liquid epoxy resin (Mitsubishi Chemical Corporation, jER-807)
  • Phenol curing agent Novolac type phenol resin (manufactured by DIC, TD-2090-60M, 60% (w / v) methyl ethyl ketone solution)
  • Amine curing agent 3,3′-diethyl-4,4′-diaminodiphenylmethane (manufactured by Nippon Kayaku Co., Ltd., Kayahard AA)
  • Phenoxy resin manufactured by Mitsubishi Chemical Corporation, YX6954BH30, 30% (w / v) methyl ethyl ketone / anone solution
  • polyvinyl acetal resin manufactured by Sekisui Chemical Co., Ltd., KS-10 (hydroxyl group 25 mol%)
  • Curing catalyst 2-ethyl-4-methylimidazole (manufactured by Shikoku Kasei Co., Ltd., 2E4MZ)
  • Coupling agent N-phenyl-3-aminopropyltrimethoxysilane (
  • Example 1 (1) Preparation of varnish 30 parts by weight of dicyclopentadiene type epoxy resin (manufactured by DIC, HP-7200) as epoxy resin, 3 parts by weight of bisphenol F type liquid epoxy resin (manufactured by Mitsubishi Chemical Corporation, jER807), phenol as cyanate resin 14 parts by weight of a novolac-type cyanate resin (manufactured by LONZA, Primaset PT-30), 3 parts by weight of YX6954BH30 manufactured by Mitsubishi Chemical Co.
  • dicyclopentadiene type epoxy resin manufactured by DIC, HP-7200
  • bisphenol F type liquid epoxy resin manufactured by Mitsubishi Chemical Corporation, jER807
  • phenol as cyanate resin 14 parts by weight of a novolac-type cyanate resin (manufactured by LONZA, Primaset PT-30)
  • YX6954BH30 manufactured by Mitsubishi Chemical Co.
  • a glass woven fabric (manufactured by Unitika Ltd., cross type # 1017, width 530 mm, thickness 15 ⁇ m, basis weight 12 g / m 2 ) was used as a fiber substrate, and the prepreg was prepared by a vacuum laminator and a hot air dryer. Manufactured. Specifically, the resin sheet 1 and the resin sheet 2 are overlapped on both sides of the glass woven fabric so that they are positioned at the center in the width direction of the glass woven fabric, respectively, and under reduced pressure conditions of 0.1 MPa (750 Torr), It joined using the 80 degreeC laminate roll.
  • 0.1 MPa 750 Torr
  • the resin layers of the resin sheet 1 and the resin sheet 2 are respectively bonded to both sides of the fiber cloth, and in the outer region of the width direction dimension of the glass woven fabric.
  • the resin layers of the resin sheet 1 and the resin sheet 2 were joined together.
  • the joined material is heated for 2 minutes through a horizontal conveying type hot air drying apparatus set at 120 ° C. without applying pressure, and has a thickness of 40 ⁇ m (T1: 17 ⁇ m, fiber base material). : 15 ⁇ m, T2: 8 ⁇ m).
  • Example 2 (1) Preparation of varnish Prepared in the same manner as in Example 1. (2) Production of Resin Sheet A resin sheet was produced in the same manner as in Example 1 except that the resin thickness on the substrate was changed to 20.5 ⁇ m (resin sheet 1) and 13.5 ⁇ m (resin sheet 2). (3) Preparation of prepreg A glass woven fabric was prepared in the same manner as in Example 1 except that the woven cloth was changed to a cloth type # 1015 (width 530 mm, thickness 17 ⁇ m, basis weight 15 g / m 2 ).
  • Example 3 A varnish, a resin sheet, and a prepreg were prepared in the same manner as in Example 1 except that the resin composition was changed to the resin composition shown in Table 1.
  • each component represents part by weight.
  • Example 4 (1) Preparation of varnish It was prepared in the same manner as in Example 1 except that the resin composition was changed to the resin composition shown in Table 1. In Table 1, each component represents part by weight.
  • Examples 5 and 6 A varnish, a resin sheet, and a prepreg were prepared in the same manner as in Example 4 except that the resin composition was changed to the resin composition shown in Table 1.
  • each component represents part by weight.
  • Comparative Examples 1 and 2 A varnish, a resin sheet, and a prepreg were prepared in the same manner as in Example 1 except that the resin composition was changed to the resin composition shown in Table 1.
  • each component represents part by weight.
  • a prepreg was placed between the two SUS plates, heated to 171 ° C. and 1.38 MPa, and hot-plate pressed for 5 minutes (FIG. 2B).
  • the release film is peeled off, and the prepreg is cut out into a columnar shape having a diameter of 81 mm so that the stacking direction of the prepreg is in the height direction (FIG. 2C), and the weight of the obtained columnar prepreg (W 2 ( g)) was measured.
  • the resin flow was determined from equation (1). The results are shown in Table 1. In the formula (1),% is% by weight.
  • Examples 1 to 4 and Comparative Examples 1 and 2 were cut into single sheets, set on the CVP300, temporarily attached to the core layer, and vacuumed at 120 ° C., 0.7 MPa for 1 minute in a vacuum laminator. Lamination was performed, followed by smoothing by hot pressing at 160 ° C., 0.55 MPa for 2 minutes. Then, it hardened
  • a fiber base and a resin layer provided on both sides of the fiber base According to IPC-TM-650 Method 2.3.17, the resin flow measured by heating and pressurizing for 5 minutes under the conditions of 171 ⁇ 3 ° C. and 1380 ⁇ 70 kPa is 15 wt% or more and 50 wt% or less. Pre-preg for build-up.
  • the prepreg is sandwiched between a pair of opposing rubber plates and heated and pressurized under the conditions of 120 ° C.
  • the resin layer contains a thermosetting resin, The build-up prepreg according to [1] or [2], wherein the thermosetting resin is selected from an epoxy resin, a cyanate resin, and a maleimide compound.
  • the resin layer includes a resin composition containing a thermosetting resin, a filler, and a curing agent.
  • the thermosetting resin is selected from an epoxy resin and a cyanate resin.
  • the resin composition contains an inorganic filler as the filler.
  • the resin composition contains a phenolic curing agent as the curing agent.
  • the build-up prepreg has a relatively thick resin layer and a relatively thin resin layer with a fiber base as a center, The laminated board according to [12], wherein the thick resin layer is laminated on the circuit forming surface.
  • a semiconductor device comprising: [15] A laminating step of laminating a prepreg for buildup on the circuit forming surface of the core layer having a circuit forming surface on one side or both sides under heat and pressure; A smoothing step of smoothing the surface of the laminated prepreg for lamination to obtain a laminate; A method of manufacturing a laminated board that continuously performs In the laminating step, heating and pressurizing the core layer and the build-up prepreg between a pair of opposing metal plates, A method for producing a laminated board, wherein the buildup prepreg according to any one of [1] to [11] is used as the buildup prepreg.
  • the build-up prepreg is wound and laminated in a roll shape, The method for producing a laminated board according to [15], wherein the build-up prepreg wound and laminated is conveyed, a sheet-like core layer is conveyed, and the laminating step and the smoothing step are continuously performed. . [17] The method for manufacturing a laminated board according to [16], wherein in the smoothing step, heating and pressurization are performed in a state where the core layer and the buildup prepreg are sandwiched between a pair of opposing plate-like elastic bodies.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Reinforced Plastic Materials (AREA)
  • Laminated Bodies (AREA)

Abstract

L'imvention concerne un préimprégné (1) pour circuit multicouche, qui comporte un substrat de fibre (2) pourvu d'une couche de résine, formée sur les deux faces de celui-ci. Conformément au procédé 2.3.17 d'IPC-TM-650, le flux de résine du préimprégné, mesuré après chauffage et pressage pendant 5 minutes dans des conditions de température de 171±3°C pour une pression de 1380±70kPa, est d'au moins 15% en poids et de 50% en poids au maximum.
PCT/JP2012/001685 2011-03-14 2012-03-12 Préimprégné pour circuit multicouche WO2012124307A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN2012800133337A CN103444276A (zh) 2011-03-14 2012-03-12 积层用预浸料
KR1020137026779A KR101907713B1 (ko) 2011-03-14 2012-03-12 빌드업용 프리프레그

Applications Claiming Priority (4)

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JP2011055195A JP5579642B2 (ja) 2011-03-14 2011-03-14 積層板の製造方法
JP2011055198A JP5547678B2 (ja) 2011-03-14 2011-03-14 積層板の製造方法
JP2011-055195 2011-03-14
JP2011-055198 2011-03-14

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WO2012124307A1 true WO2012124307A1 (fr) 2012-09-20

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Cited By (1)

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WO2016088743A1 (fr) * 2014-12-01 2016-06-09 三菱瓦斯化学株式会社 Feuille de résine, et carte de circuit imprimé

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CN110719694B (zh) * 2019-09-17 2021-07-02 沪士电子股份有限公司 一种含聚苯醚印制电路板化学镍金表面处理的方法
TW202128418A (zh) * 2019-09-30 2021-08-01 日商太陽油墨製造股份有限公司 積層結構
JP7264194B2 (ja) * 2020-06-25 2023-04-25 味の素株式会社 樹脂組成物

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EP1457515A4 (fr) * 2001-08-31 2004-11-24 Sumitomo Bakelite Co Composition de resine, preimpregne, feuille laminee, et boitier de semi-conducteur
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EP1647576A1 (fr) * 2005-04-01 2006-04-19 Huntsman Advanced Materials (Switzerland) GmbH Composition comprenant une résine epoxyde et de benzoxazine
JP2008244189A (ja) * 2007-03-28 2008-10-09 Sumitomo Bakelite Co Ltd 回路基板および半導体装置
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JP2003342399A (ja) * 2002-05-28 2003-12-03 Matsushita Electric Works Ltd プリプレグ及びこのプリプレグを用いてなる内層回路入り積層板

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WO2016088743A1 (fr) * 2014-12-01 2016-06-09 三菱瓦斯化学株式会社 Feuille de résine, et carte de circuit imprimé
JPWO2016088743A1 (ja) * 2014-12-01 2017-09-07 三菱瓦斯化学株式会社 樹脂シート及びプリント配線板

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TWI491323B (zh) 2015-07-01
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KR101907713B1 (ko) 2018-10-12
CN103444276A (zh) 2013-12-11

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